-- Nxera Pharma(東京證券交易所代碼:4565)週一在東京證券交易所提交的文件顯示,其合作夥伴Neurocrine Biosciences已完成一項實驗性精神分裂症治療藥物中期臨床試驗的首例患者給藥,觸發了Nexera向這家日本製藥商支付2250萬美元的里程碑付款。 這項第二期臨床試驗將評估NBI-1117570的療效,這是一種由Nxera研發的口服雙毒蕈鹼M1/M4受體激動劑,用於治療需要住院治療的成年精神分裂症患者。 Nxera表示,這筆款項將在2026財年第一季計入收入。 這項隨機、雙盲、安慰劑對照試驗預計將招募約120名患者。其主要目標是測量陽性與陰性症狀量表(PANSS)總分的變化,PANSS是評估症狀嚴重程度的標準工具,同時也將追蹤藥物的安全性和耐受性。 NBI-1117570靶向大腦中的毒蕈鹼型乙醯膽鹼受體,其中M1受體與認知功能相關,M4受體與精神病相關。該化合物利用Nxera公司的NxWave藥物發現平台開發,目前正與Neurocrine公司進行多專案合作,推動其研發進程。
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